Category Archives: China Food and Drug Administration

China Food and Drug Administration Minister Bi Jingquan meets the European Commission delegation

CFDA. On the afternoon of June 1, 2016, Bi Jingquan, Minister of China Food and Drug Administration (CFDA), met with the European Commission delegation headed by Mr. Phil Hogan, European Commissioner for Agriculture and Rural Development, and Mr. Hans Dietmar Schweisgut, Ambassador of the European Union to China. Both sides exchanged opinions on the revision of the Food Safety Law

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China Food and Drug Administration releases 2015 Annual Report for National Medical Device Adverse Event Monitoring

2016-05-27. China Food and Drug Administration (CFDA) recently released the 2015 Annual Report for National Medical Device Adverse Event Monitoring, which includes the general situation of medical device adverse event reporting, the statistical analysis of medical device adverse events, and the control measures for the safety risks of medical X-ray angiography equipment, external defibrillator and low frequency electromagnetic therapy equipment. The

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China Food and Drug Administration promulgates 186 industry standards for medical devices

CFDA. 2016-05-03. China Food and Drug Administration (CFDA) recently issued the No. 25 and No. 74 Announcement of 2016, which released 186 industry standards for medical devices. These standards include 42 mandatory industry standards and 144 recommended industry standards, involving implants for surgery, disinfection equipment, medical extracorporeal circulation equipment, dental equipment, ophthalmic equipment etc. The promulgation and implementation of these standards

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CFDA Vice Minister Sun Xianze attends CAE-ATSE Workshop on Technology Advances in Food Safety

2016-04-22. On the morning of April 19, 2016, Sun Xianze, Vice Minister of China Food and Drug Administration (CFDA), attended the CAE-ATSE Workshop on Technology Advances in Food Safety jointly held by Chinese Academy of Engineering (CAE) and Australian Academy of Technological Sciences and Engineering (ATSE) and delivered a speech. A total of about 130 people, including CAE President Zhou

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China Food and Drug Administration (CFDA) releases 2015 Annual Report for Medical Device Registration

2016-04-05 China Food and Drug Administration (CFDA) recently released the 2015 Annual Report for Medical Device Registration, which includes the overview of medical device registration in 2015, acceptance of medical device registration application, review and approval of china registration, review and approval of innovative medical device, and other information. Original

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Session on Drug Review and Approval held during Boao Forum for Asia Annual Conference

2016-03-25. On the morning of March 23, 2016, during the Boao Forum for Asia Annual Conference 2016, the Session on Drug Review and Approval, with the theme of “cracking down on counterfeiting, improving drug quality, promoting drug review and approval system reform & drug innovation”, was held at Boao International Conference Center. The Session was sponsored by China Food and Drug

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CFDA and NHFPC jointly issue the Good Clinical Practice for medical devices

CFDA. In order to further strengthen the supervision and management of clinical trials of medical devices, China Food and Drug Administration (CFDA) and National Health and Family Planning Commission of China (NHFPC) recently jointly issued the Good Clinical Practice for medical devices (CFDA Order No. 25), which will be implemented as of June 1, 2016. The Good Clinical Practice for medical

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Chinese drug regulator vows to fix vaccine distribution loopholes

Updated: Mar 23,2016 5:05 PM     Xinhua. BOAO — A senior Chinese drug regulator stressed strict measures to fix the loopholes in the country’s vaccine distribution system on March 23. Shandong police announced last month that they had arrested a mother and daughter suspected of illegally selling improperly stored or expired vaccines worth more than 570 million yuan ($88 million), involving 20

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CFDA issues Provisions for Registration of Foods for Special Medical Purposes

CFDA. In order to implement the Food Safety Law, standardize the registration of foods for special medical purposes, ensure the safety of foods for special medical purposes, the Provisions for Registration of Foods for Special Medical Purposes was promulgated on March 7, 2016 as CFDA Order No. 24. The Provisions will come into force as of July 1, 2016. Original

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Meeting of the EU-China Working Group on Pharmaceuticals held in Beijing

CFA2016-03-10. On the morning of March 9, 2016, Meeting of the EU-China Working Group on Pharmaceuticals was held in Beijing. The delegation of China Food and Drug Administration(CFDA)had a meeting with the European Commission delegation headed by Mr. Andrzej RYS, director of DG SANTE of the European Commission, and Mr. Guido RASI, executive director of the European Medicines Agency (EMA).

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